Arthrex Gemini™ SR8 Self-Retaining Cannula System with Disposable Cannulated Obturator and No-Squirt Cap 8.25 mm I.D. x 9 cm - FDA Registration MDR-07809

Access comprehensive regulatory information for Arthrex Gemini™ SR8 Self-Retaining Cannula System with Disposable Cannulated Obturator and No-Squirt Cap 8.25 mm I.D. x 9 cm in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number MDR-07809 and manufactured by Arthrex, Inc. - 1370 Creekside Boulevard, Naples,Florida 34108-1945 USA mfd. by: Frantz Medical Development Ltd. - 7740 Metric Drive, Mentor, OH 44060, USA in USA. The device was registered on June 30, 2025.

This page provides complete registration details including manufacturer information, importer/distributor details (PacificSurgical, Inc.), and regulatory compliance data from the official Philippines FDA medical device database. Pure Global AI offers free access to Philippines' complete medical device registry, helping global MedTech companies navigate FDA regulations efficiently.